Canonical Allele Identifier: CA1322147840
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688625063
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203866188G>T , CM000664.2:g.203866188G>T GRCh38
NC_000002.11:g.204730911G>T , CM000664.1:g.204730911G>T GRCh37
NC_000002.10:g.204439156G>T NCBI36
NG_011502.1:g.3403G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.48-1730G>T ENSP00000512655.1:n.48-1730G>T
Search 100 bp 5'
Search 100 bp 3'